Napsin a expression across subtypes of thyroid carcinoma: an immunohistochemical diagnostic encounter with prognostic correlates

Napsin a expression across subtypes of thyroid carcinoma: an immunohistochemical diagnostic encounter with prognostic correlates

Authors

  • Heba Sheta Pathology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt
  • Maha M. Fawzy Pathology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt
  • Amal Abd El hafez Pathology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt; Faculty of Medicine, Horus University-Egypt (HUE), New Damietta, Egypt
  • Amr Hossam Surgical Oncology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt
  • Sherihan I. Gouda Internal Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt
  • Ahmad Darwish Pediatric Hematology, Oncology and Bone Marrow Transplantation Unit, Pediatrics Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt
  • Doaa Sh. Alemam Public Health and Community Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt
  • Reham Alghandour Medical Oncology Unit, Oncology Center-Mansoura University (OCMU), Faculty of Medicine, Mansoura University, Mansoura, Egypt
  • Doaa H. Sakr Medical Oncology Unit, Oncology Center-Mansoura University (OCMU), Faculty of Medicine, Mansoura University, Mansoura, Egypt

Keywords:

Thyroid carcinoma, Napsin A, Frequency, Therapy, Prognosis

Abstract

Background and aim: Novel aspartic proteinase of pepsin family A (Napsin A) is a diagnostic marker for pulmonary adenocarcinoma. Recently, it was detected in carcinomas of various organs including thyroid carcinomas (TCs), raising a diagnostic challenge especially when combined with positive thyroid transcription factor-1 (TTF-1). Methods: This retrospective study investigates the frequency of Napsin A immunohistochemical (IHC) expression across subtypes of TC focusing on its association with the prognostic parameters. Sixty-three TC patients who underwent thyroidectomy were enrolled. After collecting the clinicopathological, laboratory, surgical, therapeutic and survival data, IHC was applied to TC tissue microarray-prepared sections using anti-Napsin A. IHC scoring divided TCs as: Napsin A positive & negative. Statistical and survival analyses were performed using SPSS version 26. Results: Napsin A was expressed in 17.5% of TCs with 100% expression in anaplastic TC and 19.5% expression in papillary TC. Other TC subtypes were negative. Statistically significant associations were noticed between Napsin A and some less favorable TC prognostic variables as the involvement of both lobes, anaplastic histopathology, larger tumor size, higher pathological stage, and a shorter mean OS and DFS of patients (all P ≤0.05). Conclusions: Napsin A is predominately expressed in anaplastic and papillary TC subtypes. In patients with a possible metastatic lung carcinoma or malignancy of unknown origin co-expressing Napsin A and TTF-1, the diagnosis of TC should be considered and supported with a panel of other TC markers. Considering its less favorable prognostic associations, Napsin A may be added as a molecular marker for TC risk stratification, and treatment targeting. However, the other subtypes must be evaluated in a larger series to support these conclusions. 

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Published

28-08-2024

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Section

ORIGINAL CLINICAL RESEARCH

How to Cite

1.
Sheta H, Maha M. Fawzy, Abd El hafez A, et al. Napsin a expression across subtypes of thyroid carcinoma: an immunohistochemical diagnostic encounter with prognostic correlates. Acta Biomed. 2024;95(4):e2024067. doi:10.23750/abm.v95i4.15474